Search results for "lcsh:Organic chemistry"

showing 10 items of 438 documents

Direct Analysis of Psilocin and Muscimol in Urine Samples Using Single Drop Microextraction Technique In-Line with Capillary Electrophoresis

2020

The fully automated system of single drop microextraction coupled with capillary electrophoresis (SDME-CE) was developed for in-line preconcentration and determination of muscimol (MUS) and psilocin (PSC) from urine samples. Those two analytes are characteristic active metabolites of Amanita and Psilocybe mushrooms, evoking visual and auditory hallucinations. Study analytes were selectively extracted from the donor phase (urine samples, pH 4) into the organic phase (a drop of octanol layer), and re-extracted to the acidic acceptor (background electrolyte, BGE), consisting of 25 mM phosphate buffer (pH 3). The optimized conditions for the extraction procedure of a 200 &micro

OctanolAnalyteLiquid Phase MicroextractionCalibration curveAmanitacapillary electrophoresisPharmaceutical ScienceElectrolyteUrinesingle drop microextraction01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-44103 medical and health scienceschemistry.chemical_compound0302 clinical medicineCapillary electrophoresislcsh:Organic chemistryLimit of DetectionDrug DiscoverymedicineHumans030216 legal & forensic medicinePhysical and Theoretical ChemistrypsilocinChromatographyChemistrygreen chemistry010401 analytical chemistryOrganic ChemistryElectrophoresis CapillaryHydrogen-Ion ConcentrationmuscimolurinePsilocybin0104 chemical sciencesDilutionChemistry (miscellaneous)PsilocinCalibrationHallucinogensSolventsMolecular MedicinePsilocybemedicine.drugMolecules
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Tandem cross enyne metathesis (CEYM)–intramolecular Diels–Alder reaction (IMDAR). An easy entry to linear bicyclic scaffolds

2015

A new tandem cross enyne metathesis (CEYM)–intramolecular Diels–Alder reaction (IMDAR) has been carried out. It involves conjugated ketones, esters or amides bearing a remote olefin and aromatic alkynes as the starting materials. The overall process enables the preparation of a small family of linear bicyclic scaffolds in a very simple manner with moderate to good levels of diastereoselectivity. This methodology constitutes one of the few examples that employ olefins differently than ethylene in tandem CEYM–IMDAR protocols.

Olefin fiberBicyclic moleculeTandemChemistryOrganic ChemistryConjugated systemEnyne metathesisCombinatorial chemistryFull Research Paperlcsh:QD241-441Chemistrylcsh:Organic chemistryCascade reactionDiels–Alder reactionIntramolecular forcebicyclic frameworkscross enyne metathesisOrganic chemistrylcsh:Qtandem reactionlcsh:ScienceDiels-Alder reactionDiels–Alder reactionBeilstein Journal of Organic Chemistry
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Nopal Cactus (Opuntia ficus-indica) as a Source of Bioactive Compounds for Nutrition, Health and Disease

2014

Opuntia ficus-indica, commonly referred to as prickly pear or nopal cactus, is a dicotyledonous angiosperm plant. It belongs to the Cactaceae family and is characterized by its remarkable adaptation to arid and semi-arid climates in tropical and subtropical regions of the globe. In the last decade, compelling evidence for the nutritional and health benefit potential of this cactus has been provided by academic scientists and private companies. Notably, its rich composition in polyphenols, vitamins, polyunsaturated fatty acids and amino acids has been highlighted through the use of a large panel of extraction methods. The identified natural cactus compounds and derivatives were shown to be e…

Opuntia ficus-indicaOpuntia ficusAnti-Inflammatory AgentsPharmaceutical ScienceDiseaseReviewHealth benefitsBiologyAntioxidantsAnalytical Chemistrylcsh:QD241-441lcsh:Organic chemistryDrug DiscoveryBotanycell signalingAnimalsHumansPhysical and Theoretical Chemistryanti-inflammatorychemistry.chemical_classificationPEARPlant ExtractsOrganic ChemistryOpuntiaPolyphenolschemistryChemistry (miscellaneous)CactusMolecular MedicineExtraction methodsDrug Screening Assays AntitumorPolyunsaturated fatty acidMolecules
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Stereoselective cathodic synthesis of 8-substituted (1R,3R,4S)-menthylamines.

2015

The electrochemical generation of menthylamines from the corresponding menthone oximes equipped with an additional substituent in position 8 is described. Due to 1,3-diaxial interactions a pronounced diastereoselectivity for the menthylamines is found.

Organic ChemistrySubstituentoximesElectrochemistryElectrosynthesisCombinatorial chemistryMenthonementhylaminesFull Research PaperCathodic protectionlcsh:QD241-441chemistry.chemical_compoundChemistryelectrosynthesislcsh:Organic chemistrychemistryOrganic chemistrylcsh:QStereoselectivitylcsh:Sciencecathodic reductionchiral aminesBeilstein journal of organic chemistry
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A New Benzopyranyl Cadenane Sesquiterpene and Other Antiplasmodial and Cytotoxic Metabolites from Cleistochlamys kirkii

2019

Phytochemical investigations of ethanol root bark and stem bark extracts of Cleistochlamys kirkii (Benth.) Oliv. (Annonaceae) yielded a new benzopyranyl cadinane-type sesquiterpene (cleistonol, 1) alongside 12 known compounds (2&ndash

Organisk kemibenzopyranyl sesquiterpenesyöpähoidotCleistochlamys kirkiiOrganic ChemistrymalariaAnnonaceaecleistonol<i>Cleistochlamys kirkii</i>antiplasmodial activityluonnonaineetArticlelcsh:QD241-441terpeenitlcsh:Organic chemistrylääkekemiacytotoxicityMolecules
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Possible Transmission Flow of SARS-CoV-2 Based on ACE2 Features

2020

Angiotensin-converting enzyme 2 (ACE2) is the cellular receptor for the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) that is engendering the severe coronavirus disease 2019 (COVID-19) pandemic. The spike (S) protein receptor-binding domain (RBD) of SARS-CoV-2 binds to the three sub-domains viz. amino acids (aa) 22&ndash

Pan troglodytesvirusesProtein domainACE2Pharmaceutical ScienceBiologyArticleAnalytical Chemistrylcsh:QD241-44103 medical and health sciencesDogs0302 clinical medicineProtein DomainsSpecies Specificitylcsh:Organic chemistryDrug DiscoveryAnimalsHumansviral spike receptor-binding domainPhysical and Theoretical ChemistryReceptor030304 developmental biologychemistry.chemical_classification0303 health sciencesCATSSARS-CoV-2Transmission (medicine)fungiOrganic ChemistrytransmissionCOVID-19virus diseasesbioinformaticsMetabolismVirologyAmino acidEnzymechemistryChemistry (miscellaneous)030220 oncology & carcinogenesisSpike Glycoprotein CoronavirusAngiotensin-converting enzyme 2CatsMolecular MedicineCattleAngiotensin-Converting Enzyme 2hormones hormone substitutes and hormone antagonistsMolecules
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Water-Dependent Blending of Pectin Films: The Mechanics of Conjoined Biopolymers

2020

Biodegradable pectin polymers have been recommended for a variety of biomedical applications, ranging from the delivery of oral drugs to the repair of injured visceral organs. A promising approach to regulate pectin biostability is the blending of pectin films. To investigate the development of conjoined films, we examined the physical properties of high-methoxyl pectin polymer-polymer (homopolymer) interactions at the adhesive interface. Pectin polymers were tested in glass phase (10&ndash

PectinPharmaceutical Science02 engineering and technology01 natural sciencesAnalytical ChemistryDiffusionBiopolymersTheoretical and Computational ChemistryPhase (matter)Drug DiscoveryComposite materialchemistry.chemical_classificationpectindigestive oral and skin physiologyfood and beveragesPolymerAdhesion021001 nanoscience & nanotechnologyCompressive strengthChemistry (miscellaneous)ArtificialMolecular MedicinePectins0210 nano-technologyscanning electron microscopyanimal structuresfood.ingredientMaterials sciencehomopolymer adhesionmacromolecular substances010402 general chemistrycomplex mixturesPaint adhesion testingArticlelcsh:QD241-441Medicinal and Biomolecular Chemistryfoodlcsh:Organic chemistryPolysaccharidesUltimate tensile strengthPhysical and Theoretical ChemistryMembranesOrganic ChemistryWaterMembranes Artificial0104 chemical scienceschemistryfracture mechanicspolysaccharideAdhesiveGlassGelsMolecules
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Molecular Classification of Pesticides Including Persistent Organic Pollutants, Phenylurea and Sulphonylurea Herbicides

2014

Pesticide residues in wine were analyzed by liquid chromatography–tandem mass spectrometry. Retentions are modelled by structure–property relationships. Bioplastic evolution is an evolutionary perspective conjugating effect of acquired characters and evolutionary indeterminacy–morphological determination–natural selection principles; its application to design co-ordination index barely improves correlations. Fractal dimensions and partition coefficient differentiate pesticides. Classification algorithms are based on information entropy and its production. Pesticides allow a structural classification by nonplanarity, and number of O, S, N and Cl atoms and cycles; different behaviours depend …

Periodic table (large cells)periodic law; periodic property; periodic table; molecular classificationperiodic tablePharmaceutical ScienceWineFractal dimensionArticleAnalytical Chemistrylcsh:QD241-441lcsh:Organic chemistryTandem Mass SpectrometryDrug DiscoveryPesticidesPhysical and Theoretical ChemistryPollutantChromatographyMolecular Structuremolecular classificationChemistryOrganic ChemistryPesticide Residuesperiodic lawPesticideperiodic propertyStatistical classificationSulfonylurea CompoundsCategorizationChemistry (miscellaneous)Principal component analysisMolecular MedicineBiological systemCombinatorial explosionChromatography LiquidMolecules; Volume 19; Issue 6; Pages: 7388-7414
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Euphosantianane E–G: Three New Premyrsinane Type Diterpenoids from Euphorbia sanctae-catharinae with Contribution to Chemotaxonomy

2019

Euphorbia species were widely used in traditional medicines for the treatment of several diseases. From the aerial parts of Egyptian endemic plant, Euphorbia sanctae-catharinae, three new premyrsinane diterpenoids, namely, euphosantianane E&ndash

Pharmaceutical ScienceAgglomerative hierarchical clustering01 natural sciencesArticlepremyrsinane diterpenoidsAnalytical Chemistrylcsh:QD241-441TerpeneType (biology)lcsh:Organic chemistryEuphorbiaDrug DiscoveryPhysical and Theoretical ChemistryEuphorbiaMolecular StructurebiologyTraditional medicinePlant Extracts010405 organic chemistryOrganic ChemistryeuphorbiaceaeEuphorbiaceaeEuphorbia sanctae-catharinaePlant Components Aerialendemic plantchemotaxonomic significancebiology.organism_classificationAntineoplastic Agents Phytogenic0104 chemical sciences010404 medicinal & biomolecular chemistryChemistry (miscellaneous)Chemotaxonomyeuphosantianane E–G<i>Euphorbia sanctae-catharinae</i>Molecular MedicineEgyptDiterpenesDrug Screening Assays AntitumorMolecules
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Chemical Composition and Possible in Vitro Phytotoxic Activity of Helichrsyum italicum (Roth) Don ssp. italicum

2011

The chemical composition of the essential oil of Helichrysum italicum (Roth) Don ssp. italicum, collected in the National Park of Cilento and Diano Valley, Southern Italy, was studied by means of GC and GC/MS. Forty four compounds of 45 constituents were identified in the oil, mainly oxygenated sesquiterpenes. The essential oil was evaluated for its potential in vitro phytotoxic activity against germination and early radicle elongation of radish and garden cress. The radicle elongation of radish was significantly inhibited at the highest doses tested, while germination of both seeds was not affected.

Pharmaceutical ScienceGerminationphytotoxicityHelichrysum italicum (Roth) Don ssp. italicumPlant RootsHelichrysum italicumArticleLepidium sativumessential oilRaphanusAnalytical Chemistrylaw.inventionlcsh:QD241-441lcsh:Organic chemistrylawDrug DiscoveryBotanyOils VolatileRadiclePhysical and Theoretical ChemistryChemical compositionEssential oilHelichrysumbiologyHerbicidesPlant ExtractsOrganic Chemistryfood and beverages<em>Helichrysum italicum </em>(Roth) Don ssp.<em> italicum</em>; essential oil; phytotoxicitybiology.organism_classificationChemistry (miscellaneous)GerminationMolecular MedicinePhytotoxicitySesquiterpenesMolecules; Volume 16; Issue 9; Pages: 7725-7735
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